FIBERGRAFT BG PUTTY BONE GRAFT SUBSTITUTE

FIBERGRAFT BG PUTTY BONE GRAFT SUBSTITUTE is an FDA 510(k)-cleared medical device (K143533) manufactured by Prosidyan, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 24, 2015. Regulation: 8.